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Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex

Although multisensory integration is crucial for sensorimotor function, it is unclear how visual and proprioceptive sensory cues are combined in the brain during motor behaviors. Here we characterized the effects of multisensory interactions on local field potential (LFP) activity obtained from the...

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Autores principales: VanGilder, Paul, Shi, Ying, Apker, Gregory, Buneo, Christopher A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079385/
https://www.ncbi.nlm.nih.gov/pubmed/33907213
http://dx.doi.org/10.1038/s41598-021-88278-5
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author VanGilder, Paul
Shi, Ying
Apker, Gregory
Buneo, Christopher A.
author_facet VanGilder, Paul
Shi, Ying
Apker, Gregory
Buneo, Christopher A.
author_sort VanGilder, Paul
collection PubMed
description Although multisensory integration is crucial for sensorimotor function, it is unclear how visual and proprioceptive sensory cues are combined in the brain during motor behaviors. Here we characterized the effects of multisensory interactions on local field potential (LFP) activity obtained from the superior parietal lobule (SPL) as non-human primates performed a reaching task with either unimodal (proprioceptive) or bimodal (visual-proprioceptive) sensory feedback. Based on previous analyses of spiking activity, we hypothesized that evoked LFP responses would be tuned to arm location but would be suppressed on bimodal trials, relative to unimodal trials. We also expected to see a substantial number of recording sites with enhanced beta band spectral power for only one set of feedback conditions (e.g. unimodal or bimodal), as was previously observed for spiking activity. We found that evoked activity and beta band power were tuned to arm location at many individual sites, though this tuning often differed between unimodal and bimodal trials. Across the population, both evoked and beta activity were consistent with feedback-dependent tuning to arm location, while beta band activity also showed evidence of response suppression on bimodal trials. The results suggest that multisensory interactions can alter the tuning and gain of arm position-related LFP activity in the SPL.
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spelling pubmed-80793852021-04-28 Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex VanGilder, Paul Shi, Ying Apker, Gregory Buneo, Christopher A. Sci Rep Article Although multisensory integration is crucial for sensorimotor function, it is unclear how visual and proprioceptive sensory cues are combined in the brain during motor behaviors. Here we characterized the effects of multisensory interactions on local field potential (LFP) activity obtained from the superior parietal lobule (SPL) as non-human primates performed a reaching task with either unimodal (proprioceptive) or bimodal (visual-proprioceptive) sensory feedback. Based on previous analyses of spiking activity, we hypothesized that evoked LFP responses would be tuned to arm location but would be suppressed on bimodal trials, relative to unimodal trials. We also expected to see a substantial number of recording sites with enhanced beta band spectral power for only one set of feedback conditions (e.g. unimodal or bimodal), as was previously observed for spiking activity. We found that evoked activity and beta band power were tuned to arm location at many individual sites, though this tuning often differed between unimodal and bimodal trials. Across the population, both evoked and beta activity were consistent with feedback-dependent tuning to arm location, while beta band activity also showed evidence of response suppression on bimodal trials. The results suggest that multisensory interactions can alter the tuning and gain of arm position-related LFP activity in the SPL. Nature Publishing Group UK 2021-04-27 /pmc/articles/PMC8079385/ /pubmed/33907213 http://dx.doi.org/10.1038/s41598-021-88278-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
VanGilder, Paul
Shi, Ying
Apker, Gregory
Buneo, Christopher A.
Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex
title Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex
title_full Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex
title_fullStr Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex
title_full_unstemmed Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex
title_short Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex
title_sort sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079385/
https://www.ncbi.nlm.nih.gov/pubmed/33907213
http://dx.doi.org/10.1038/s41598-021-88278-5
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